Canonical Allele Identifier: PA2830263879
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1470326
ClinVar RCV Id: RCV001973242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ser296Thr
CA398533085
NM_144997.7:c.886T>A